Canonical Allele Identifier: CA413704598

Gene: ATRX

Linked Data

• dbSNP Id: rs2147650422
• MyVariant Identifiers: chrX:g.76764004T>C (hg19) ; chrX:g.77508526T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508526T>C , CM000685.2:g.77508526T>C	GRCh38
NC_000023.10:g.76764004T>C , CM000685.1:g.76764004T>C	GRCh37
NC_000023.9:g.76650660T>C	NCBI36
NG_008838.2:g.282696A>G
NG_008838.3:g.282744A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7304A>G MANE Select	ENSP00000362441.4:p.His2435Arg
ENST00000675732.1:c.2402A>G	ENSP00000502598.1:p.His801Arg
ENST00000373344.9:c.7304A>G	ENSP00000362441.4:p.His2435Arg
ENST00000395603.7:c.7190A>G	ENSP00000378967.3:p.His2397Arg
ENST00000480283.5:c.*6932A>G	ENSP00000480196.1:n.*6932A>G
ENST00000623706.3:n.5624A>G
ENST00000624766.1:n.535A>G
NM_000489.4:c.7304A>G	NP_000480.3:p.His2435Arg
NM_138270.3:c.7190A>G	NP_612114.2:p.His2397Arg
XM_005262153.3:c.7301A>G	XP_005262210.2:p.His2434Arg
XM_005262154.3:c.7217A>G	XP_005262211.2:p.His2406Arg
XM_005262155.3:c.7187A>G	XP_005262212.2:p.His2396Arg
XM_005262156.3:c.7139A>G	XP_005262213.2:p.His2380Arg
XM_005262157.3:c.7100A>G	XP_005262214.2:p.His2367Arg
XM_006724666.2:c.7187A>G	XP_006724729.1:p.His2396Arg
XM_006724667.2:c.7025A>G	XP_006724730.1:p.His2342Arg
XR_938400.1:n.8896A>G
NM_000489.5:c.7304A>G	NP_000480.3:p.His2435Arg
XM_005262153.5:c.7301A>G	XP_005262210.2:p.His2434Arg
XM_005262154.5:c.7217A>G	XP_005262211.2:p.His2406Arg
XM_005262155.4:c.7187A>G	XP_005262212.2:p.His2396Arg
XM_005262156.4:c.7139A>G	XP_005262213.2:p.His2380Arg
XM_005262157.5:c.7100A>G	XP_005262214.2:p.His2367Arg
XM_006724666.4:c.7187A>G	XP_006724729.1:p.His2396Arg
XM_006724667.3:c.7025A>G	XP_006724730.1:p.His2342Arg
XM_017029601.2:c.7214A>G	XP_016885090.1:p.His2405Arg
XM_017029602.1:c.7184A>G	XP_016885091.1:p.His2395Arg
XM_017029603.1:c.7136A>G	XP_016885092.1:p.His2379Arg
XM_017029604.2:c.7103A>G	XP_016885093.1:p.His2368Arg
XM_017029605.1:c.7100A>G	XP_016885094.1:p.His2367Arg
XM_017029606.2:c.7073A>G	XP_016885095.1:p.His2358Arg
XM_017029607.2:c.7070A>G	XP_016885096.1:p.His2357Arg
XM_017029608.2:c.7022A>G	XP_016885097.1:p.His2341Arg
XM_017029609.1:c.6986A>G	XP_016885098.1:p.His2329Arg
XM_017029610.1:c.6983A>G	XP_016885099.1:p.His2328Arg
XM_017029611.1:c.6938A>G	XP_016885100.1:p.His2313Arg
XR_001755700.2:n.7603A>G
NM_138270.4:c.7190A>G	NP_612114.2:p.His2397Arg
NM_000489.6:c.7304A>G MANE Select	NP_000480.3:p.His2435Arg
NM_138270.5:c.7190A>G	NP_612114.2:p.His2397Arg